JP6178241B2 - 血管新生障害の処置 - Google Patents
血管新生障害の処置 Download PDFInfo
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- JP6178241B2 JP6178241B2 JP2013553604A JP2013553604A JP6178241B2 JP 6178241 B2 JP6178241 B2 JP 6178241B2 JP 2013553604 A JP2013553604 A JP 2013553604A JP 2013553604 A JP2013553604 A JP 2013553604A JP 6178241 B2 JP6178241 B2 JP 6178241B2
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WO2012109567A2 (fr) | 2011-02-11 | 2012-08-16 | The Rockefeller University | Traitement de troubles d'angiogenèse |
TWI465241B (zh) * | 2012-12-19 | 2014-12-21 | Ind Tech Res Inst | 圓柏(Juniperus chinensis)萃取物或木酚素(lignan)用於製造抑制血管新生之藥物的用途 |
HUP1300509A2 (hu) * | 2013-08-30 | 2015-03-30 | Gabor Firneisz | CXCL12 (Chemokine (C-X-C motif) Ligand 12) és IGFBP2 (Insulin-Like Growth Factor Binding Protein 2) gátlók cukorbetegséggel összefüggõ hasnyálmirigyrák kezelésénél történõ alkalmazásra |
ES2688737A1 (es) * | 2017-05-04 | 2018-11-06 | Universidad Del País Vasco / Euskal Herriko Unibertsitatea | Método para diagnosticar placa ateroesclerótica inestable |
WO2020079489A2 (fr) * | 2018-07-17 | 2020-04-23 | Helixmith Co., Ltd. | Traitement d'une neuropathie avec des constructions d'adn codant pour igf-1 et des constructions d'adn codant pour hgf |
CN111808938A (zh) * | 2019-04-11 | 2020-10-23 | 南方医科大学南方医院 | Atp6v0d2用于动脉粥样硬化的早期诊断或疗效监控 |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
DE69233482T2 (de) | 1991-05-17 | 2006-01-12 | Merck & Co., Inc. | Verfahren zur Verminderung der Immunogenität der variablen Antikörperdomänen |
ES2136092T3 (es) | 1991-09-23 | 1999-11-16 | Medical Res Council | Procedimientos para la produccion de anticuerpos humanizados. |
US5639641A (en) | 1992-09-09 | 1997-06-17 | Immunogen Inc. | Resurfacing of rodent antibodies |
AU725186B2 (en) * | 1995-11-16 | 2000-10-05 | Baylor College Of Medicine | Method for identifying metastatic sequences |
WO1999046385A2 (fr) * | 1998-03-13 | 1999-09-16 | Baylor College Of Medicine | Compositions et methodes de traitement et de prevention de troubles metastatiques |
US8257750B2 (en) | 1999-04-30 | 2012-09-04 | Kibow Biotech, Inc. | Calcium carbonate compositions for preventing or treating hyperphosphatemia |
WO2000069454A1 (fr) | 1999-05-17 | 2000-11-23 | Board Of Regents, The University Of Texas System | Suppression de l'igfbp-2 endogene visant a inhiber le cancer |
IL154529A0 (en) * | 2000-09-14 | 2003-09-17 | Univ British Columbia | Antisense insulin-like growth factor binding protein (igfep)-2-oligodeoxynucleotides for prostate and other endocrine tumor therapy |
US20040018973A1 (en) * | 2002-01-25 | 2004-01-29 | University Of Pittsburgh | Nuclear matrix protein alterations associated with colon cancer and colon metastasis to the liver, and uses thereof |
AU2003258426B2 (en) * | 2002-08-21 | 2008-04-10 | The University Of British Columbia | RNAi probes targeting cancer-related proteins |
CA2531916A1 (fr) | 2003-07-10 | 2005-02-17 | Central Institute For Experimental Animals | Modele animal utile pour l'analyse des metastases tumorales |
AU2004298604B2 (en) | 2003-12-15 | 2010-09-23 | The Regents Of The University Of California | Molecular signature of the PTEN tumor suppressor |
FR2865736B1 (fr) | 2004-02-02 | 2006-07-14 | Synt Em | Inhibiteurs de l'angiogenese, compositions les contenant et leur utilisation pour le traitement des maladies liees a une deregulation de l'angiogenese |
US20060198789A1 (en) * | 2005-01-06 | 2006-09-07 | Zhigang Weng | Target validation assay |
AU2006228989B2 (en) * | 2005-03-30 | 2012-06-14 | Murdoch Childrens Research Institute | Methods and agents for modulating cellular activity |
WO2007056604A2 (fr) * | 2005-11-09 | 2007-05-18 | Irm Llc | Procédés et compositions servant à moduler la motilité cellulaire et à inhiber la métastase de tumeurs |
WO2008073660A1 (fr) * | 2006-11-09 | 2008-06-19 | University Of Washington | Molécules et procédés pour le traitement et la détection du cancer |
KR20100102110A (ko) | 2007-11-09 | 2010-09-20 | 페레그린 파마수티컬즈, 인크 | 항-vegf 항체 조성물 및 방법 |
WO2009082744A2 (fr) * | 2007-12-22 | 2009-07-02 | Sloan-Kettering Institute For Cancer Research | Pronostic et traitement véhiculé par interférence du cancer du sein |
US9179654B2 (en) * | 2008-04-07 | 2015-11-10 | Cornell Research Foundation, Inc. | Inhibition of angiogenesis |
WO2009133141A2 (fr) * | 2008-04-29 | 2009-11-05 | Pharnext | Nouvelles approches thérapeutiques pour traiter la maladie d'alzheimer et les troubles qui lui sont associés par modulation de l'angiogenèse |
WO2009154790A2 (fr) * | 2008-06-20 | 2009-12-23 | University Of Massachusetts | Nouveaux gènes suppresseurs de métastase et utilisations associés |
WO2010064702A1 (fr) * | 2008-12-05 | 2010-06-10 | 国立大学法人 東京大学 | Biomarqueur pour prédire un pronostic de cancer |
WO2011011061A2 (fr) * | 2009-07-21 | 2011-01-27 | The Board Of Trustees Of The Leland Stanford Junior University | Procédé de régulation de l'angiogenèse et de la lymphangiogenèse, et composition pharmaceutique pour effectuer une thérapie de cancer anti-angiogénique et anti-lymphangiogénique |
WO2012109567A2 (fr) | 2011-02-11 | 2012-08-16 | The Rockefeller University | Traitement de troubles d'angiogenèse |
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